- Role
- Country
- Date of registration
- Address
NL-MF-000001489dS FLEX-S is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Philips Medical Systems Nederland B.V.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Mar 5, 2026
0884838BM913TGPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00884838118379
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
3 warnings recorded — scroll inside the panel to see all entries.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Netherlands; available across 23 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Oct 30, 2023 | Dec 31, 9999 |
| Austria | Oct 30, 2023 | Dec 31, 9999 |
| Belgium | Oct 30, 2023 | Dec 31, 9999 |
| Bulgaria | Oct 30, 2023 | Dec 31, 9999 |
| Cyprus | Oct 30, 2023 | Dec 31, 9999 |
| Germany | Oct 30, 2023 | Dec 31, 9999 |
| Denmark | Oct 30, 2023 | Dec 31, 9999 |
| Estonia | Oct 30, 2023 | Dec 31, 9999 |
| Spain | Oct 30, 2023 | Dec 31, 9999 |
| Finland | Oct 30, 2023 | Dec 31, 9999 |
| Hungary | Oct 30, 2023 | Dec 31, 9999 |
| Ireland | Oct 30, 2023 | Dec 31, 9999 |
| Iceland | Oct 30, 2023 | Dec 31, 9999 |
| Italy | Oct 30, 2023 | Dec 31, 9999 |
| Liechtenstein | Oct 30, 2023 | Dec 31, 9999 |
| Luxembourg | Oct 30, 2023 | Dec 31, 9999 |
| Latvia | Oct 30, 2023 | Dec 31, 9999 |
| Malta | Oct 30, 2023 | Dec 31, 9999 |
| Norway | Oct 30, 2023 | Dec 31, 9999 |
| Poland | Oct 30, 2023 | Dec 31, 9999 |
| Romania | Oct 30, 2023 | Dec 31, 9999 |
| Sweden | Oct 30, 2023 | Dec 31, 9999 |
| Slovenia | Oct 30, 2023 | Dec 31, 9999 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
00884838118379Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
0884838BM913TG459801729983UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1105018099MAGNETIC RESONANCE (MR) SYSTEMS - HARDWARE ACCESSORIES - OTHERZ1105018002MAGNETIC RESONANCE (MR) RADIOFREQUENCY VOLUMETRIC COILSZ1105018001MAGNETIC RESONANCE (MR) RADIOFREQUENCY SURFACE COILSCertificate health across this manufacturer's portfolio.
HZ 1135905-1SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →No certificate specifically references this device's Basic UDI-DI.